Model 3011A Uropump III Operators Manual Rev B

Table of Contents Introduction ...3 General Description...3 Formatting Conventions Used in this Manual ...3 Illustrations in this Manual ...3 Contact Information ...4 Precautions...4 Safety ...4 Environment ...6 Environmental Protection ...9 Service...10 Meaning of Symbols...10 Accessories, Cables & Supplies...13 Interface Cables ...13 Power Cords...13 Power (Jumper) Cords ...14 Optional Uropump Manual Control...15 Tubing & Tubing Sets...16 IPTS-LT2 / IPTSA-LT2 ...16 DIPTS-LT2...16 IPTS-DC-LT2...17 IT / ITA...17 IT-RT ...17 DCIT-RT ...17 Using a Tubing with Damping Chamber & Restrictor Tube ...18 Installation & System Interface...19 Unpacking Uropump III Components ...19 Attaching Uropump III to Instrument Stand ...19 System Interface Illustration ...20 Interfacing Uropump III with Life-Tech Systems or Component System Connections ...21 Disconnecting Uropump III from Remote Control Component...22 Connecting Uropump III to Power Sources...22 Using Model 3011A Uropump® III ...23 Overview of Front Panel...23 Overview of Bottom Panel...24 Preparation ...25 Operate Uropump III with Life-Tech Urodynamic System...27 Operate Uropump III with Manual Control (Model 2011CU / UMC)...28 Maintenance and Repair ...29 Introduction...29 Product Return Information ...29 Troubleshooting Guide ...30 Maintenance ...32 Cleaning & Disinfection ...33 Introduction...33 Cleaning / Disinfecting Procedure ...34 Declaration of Conformity ...35 Index ...37

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Table of Figures Figure 1 – Power Cord Connections ... 14 Figure 2 – Model 2011CU / UMC (Uropump Manual Control) ... 15 Figure 3 – Tubing & Tubing Sets ... 16 Figure 4 – Attaching Uropump III to Stand... 19 Figure 5 – Uropump III Remote Control Connections... 20 Figure 6 – Uropump III Front Panel... 23 Figure 7 – Uropump III Bottom Panel... 24 Figure 8 – Uropump III and IPTS-LT2 / IPTSA-LT2 / DIPTS-LT2 (IT / ITA) Tubing Sets ... 25 Figure 9 – Uropump III and IPTS-DC-LT2 (IT-RT, DCIT-RT) Tubing Sets... 26 Figure 10 – Using the Uropump Manual Control... 28

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Introduction General Description

Model 3011A Uropump III provides fluid infusion over a wide range of rates for cystometry, urethral pressure profilometry, and upper urinary tract studies. When interfaced to Life-Tech Urodynamic System, the Uropump III is controlled (start / end infusion and increase / decrease rate) through the urodynamic recorder’s software. The pump is attached to a Life-Tech instrument stand (or its equivalent) with the Uropump III mounting bracket. The Uropump III can be operated manually when interfaced to the optional Uropump Manual Control (Model 2011C / UMC).

Formatting Conventions Used in this Manual

WARNING CAUTION

 NOTE Carefully review the paragraph associated with any of these headings to ensure the safe and effective operation of this product. WARNING: A WARNING indicates that the personal safety of the patient or equipment operator may be involved. Disregarding a WARNING could result in injury to the patient or operator of the equipment. CAUTION: A CAUTION indicates that particular service procedures or precautions must be followed to avoid possible damage to the product.

 NOTE: A NOTE indicates special information to improve the ease of maintaining or using the product, or to clarify important information.

Illustrations in this Manual

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Some of the illustrations contained in this manual may not represent the exact construction details of the user’s specific equipment model. The illustrations in this manual are provided as general information to aid in showing possible features and components.

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Introduction, Continued Contact Information

Mailing Address:

Life-Tech, Inc. PO Box 1849 Stafford, Texas 77497-1849 United States of America

Telephone:

(281) 491-6600 (800) 231-9841

FAX:

Administrative / Financial Sales / Customer Service Technical and Clinical Support International Sales

Internet:

http://www.life-tech.com

(281) 491-6646 (281) 491-7197 (281) 491-6852 (281) 491-6852

The Life-Tech representative for the European Community is: FBI Fred Berninger Importe Bergstrasse 12 82024 Taufkirchen GERMANY Tel: +49 89 61 453 453 Fax: +49 89 61 453 455 Email: [email protected]

Precautions

WARNING: Read this instruction manual thoroughly and be familiar with its contents prior to using this equipment. Read the entire instruction manual before assembling or connecting the equipment. Take special care to follow the warnings shown on the Uropump III itself, as well as any safety suggestions in this manual.

Safety

Please read these safety instructions carefully before using this instrument. Before using the instrument, it is imperative that you be acquainted with how it operates and is controlled. 1.

WARNING: Do NOT touch the pins of the connectors marked with the symbol without following the Electrostatic Discharge (ESD) precautionary procedures detailed on page 21 of this manual. Staff that could touch the pins of the connectors identified with the ESD warning symbol should receive precautionary explanation and training. This includes clinical / biomedical engineering and healthcare staff. Electrostatic Discharge training should include an introduction to the physics of electrostatic charge, the voltage levels that can occur in normal practice and the damage that can be done to electronic components if they are touched by an operator who is electrostatically charged. Further, an explanation should be given of methods to prevent build-up of electrostatic charge, and how and why to discharge one’s body to an earth ground or to the frame of the equipment, or bond oneself by means of a wrist strap to the equipment or to an earth ground prior to making a connection.

Continued on next page… 4

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Introduction, Continued Safety (cont.)

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WARNING: To avoid risk of fire, replace the fuse(s) only as marked. WARNING: There is a risk of an explosion if the instrument is used in the presence of flammable anesthetics. 4. WARNING: The pump rollers rotate and can trap fingers, and entangle hair and/or clothing resulting in personal injuries. Keep fingers, hair and clothing out of the pump roller area while the pump is running. 5. WARNING: To reduce the risk of electrical shock, do not open the instrument’s inner housing. Refer servicing to qualified personnel only. 6. Disassembly of pump by unauthorized personnel will void the unit’s warranty. 7. WARNING: Accessory equipment connected to the analog and digital interfaces (signal inputs and signal outputs) must be certified according to the respective IEC/EN standards (i.e. IEC 60950-1/EN60950-1 for data processing equipment and IEC 60601-1/EN 60601-1 for medical equipment). Furthermore, all configurations shall comply with the system standard IEC 60601-1. Anyone who connects additional equipment to the signal input parts configures a medical system, and is therefore responsible that the system complies with the requirements of the system standard IEC 601-1. If in doubt, consult the technical service department or you local representative. 8. WARNING (only for USA) - Hospital Grade Connection: For power cords with “Hospital Grade” plugs, grounding reliability can only be achieved when the equipment is connected to an equivalent receptacle marked “Hospital Only” or "Hospital Grade.” 9. WARNING: Mount the instrument on a Life-Tech instrument stand, or an equivalent stand, no more than 2 feet (61 cm) above the floor. Mounting the device higher than 2 feet (61 cm) could affect the stability of the pole, which may inadvertently tip over and cause damage to the instrument or injury to a person in the adjacent area. Do NOT mount this equipment on an un-weighted instrument stand. 10. WARNING: Take care when moving the pump and instrument stand combination. Quick stops, excessive force and travel over uneven surfaces may cause the stand with attached devices to overturn. 11. Power Cord Connection:. Route the mains AC power supply cord so that it is not likely to be stepped on or pinched by items placed upon or against it. Never take hold of the plug or cord if your hand is wet and always grasp the plug body when connecting or disconnecting it. 12. WARNING: Do NOT disconnect the Uropump III interface cable from the M30 Module while conducting a urodynamic procedure. If the interface cable is disconnected, data recorded during the procedure is lost. 13. Power Source: Connect this device only to a mains power supply, as marked on the bottom panel. Should any liquid or solid object fall onto the pump, unplug it and have it checked by qualified personnel before operating it further. To disconnect the cord, pull it out by the plug. Never pull the cord itself. The wall outlet should be near the unit and easily accessible. The unit is not disconnected from the mains AC power source as long as it is connected to the wall outlet, even if the pump itself has been turned off. 2. 3.

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Introduction, Continued Environment

1. Water and Moisture: Do not immerse the instrument in any fluid. 2. Magnetism: Situate the instrument away from equipment or devices that generate strong magnetic fields. 3. Storage / Shipping Conditions: Humidity: 10 to 90% (non-condensing) Temperature: -4° to 140°F (-20° to 60°C) Atmospheric Pressure: 50kPa to 106kPa 4. Operating Conditions: Humidity: 30 to 75% (non-condensing) Temperature: 50° to 104°F (10° to 40°C) CAUTION: Allow adequate air circulation to prevent internal heat build-up. Do NOT install the unit in a location near heat sources such as radiators or air ducts, or in a place subject to direct sunlight, excessive dust, or humidity, mechanical vibration or shock. To avoid moisture condensation, do NOT install the unit in a location where the temperature may rise rapidly. 5. Electromagnetic Compatibility: This equipment has been tested and found to comply with the EMC limits for the Medical Device Directive 93/42 EEC (EN 55011 Class A and EN 60601-1-2:2001). These limits are designed to provide reasonable protection against harmful interference in a typical medical installation. The equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to other devices in the vicinity. However, there is no guarantee that the interference will not occur in a particular installation. If this equipment does cause harmful interference with other devices, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures: a

Reorient or relocate the receiving device.

b

Increase the separation between the equipment.

c

Connect the equipment into an outlet on a circuit different from that to which the other device(s) is connected.

d

Consult the manufacturer or field service technician for help.

Guidance and Manufacturer’s Declaration – Electromagnetic Emissions The Uropump III is intended for use in the electromagnetic environment specified below. The user of the Uropump III should assure that it is used in such an environment. Emissions test

Compliance

Electromagnetic enforcement – guidance

RF Emissions CISPR 11

Group 1

The Uropump III uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause interference in nearby electronic equipment.

RF Emissions CISPR 11

Class A

Harmonic emissions IEC 61000-3-2

Class A

Voltage fluctuations / flicker emissions IEC 61000-3-3

Complies

The Uropump III is suitable for use in all establishments other than domestic and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes.

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Introduction, Continued Environment (cont.) Guidance and Manufacturer’s Declaration – Electromagnetic Immunity The Uropump III is intended for use in the electromagnetic environment specified below. The user of the Uropump III should assure that it is used in such an environment. Electromagnetic Environment – Guidance

Immunity Test

IEC 60601 Test Level

Compliance Level

Electrostatic Discharge (ESD) IEC 61000-4-2

6Kv contact 8kV air

Test not applicable since all inputs and outputs are marked ESD sensitive and should not be touched without following the warnings on page 21 of this manual.

Electrical Fast Transient / burst IEC 61000-4-4

2Kv for power supply lines 1kV for input / output lines

1Kv for power supply lines 1kV for input / output lines

Mains power quality should be that of a typical commercial or hospital environment.

Surge IEC 61000-4-5

1Kv differential mode

1Kv differential mode

2kV common mode

2kV common mode

Mains power quality should be that of a typical commercial or hospital environment.

Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11

<5% UT (>95% dip in UT ) for 0.5 cycle 49% UT (60% dip in UT ) for 5 cycles 70% UT (30% dip in UT ) for 25 cycles 5% UT (>95% dip in UT ) for 5 sec

<5% UT (>95% dip in UT ) for 0.5 cycle 49% UT (60% dip in UT ) for 5 cycles 70% UT (30% dip in UT ) for 25 cycles 5% UT (>95% dip in UT ) for 5 sec

Mains power quality should be that of a typical commercial or hospital environment. If the user of the Uropump III requires continued operation during power mains interruptions, it is recommended that the Uropump III be powered from an uninterruptible power supply or a battery.

Power Frequency (50 / 60Hz) magnetic field IEC 610004-8

3A/m

3A/m

Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.

Note: UT = 120 / 240VAC mains voltage prior to application of the test level. Continued on next page…

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Introduction, Continued Environment (cont.) Guidance and Manufacturer’s Declaration – Electromagnetic Immunity The Uropump III is intended for use in the electromagnetic environment specified below. The user of the Uropump III should assure that it is used in such an environment. Immunity Test

Conducted RF IEC 61000-4-6 Radiated RF IEC 61000-4-3

IEC 60601 Test Level

Compliance Level

3 Vrms 150 kHz to 80 MHz

3 Vrms 150 kHz to 80 MHz

3 V/m 80 MHz to 2.5 GHz

3 V/m 80 MHz to 2.5 GHz

Electromagnetic Environment – Guidance Portable and mobile RF communications equipment should be used no closer to any part of the Uropump III, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation distance ⎡ 3.5 ⎤ d =⎢ ⎥ P ⎣ V1 ⎦

⎡ 3. 5 ⎤ d = ⎢ ⎥ P 80 MHz to 800 MHz ⎣ E1 ⎦

⎡7⎤ d = ⎢ ⎥ P 800MHz to 2.5GHz ⎣ E1 ⎦ Where P is the maximum output power where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in meters (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey,1 should be less than the compliance level in each frequency range.2 Interference may occur in the vicinity of equipment marked with the symbol.

Field strengths from fixed transmitters, such as base stations for radio (cellular / cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the Uropump III is used exceeds the applicable RF compliance level above, the Uropump III should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the Uropump III. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m. Note 1: At 80 MHz and 800 MHz, the higher frequency range applies. Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people. Continued on next page… 8

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Introduction, Continued Environment (cont.) Recommended Separation Distances Between Portable and Mobile RF Communications Equipment and the Model 3011A Uropump III The Uropump III is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The user of the Uropump III can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the Uropump III as recommended below, according to the maximum output power of the communications equipment. Separation distance according to frequency of transmitter (meters) Rated maximum output power of transmitter (Watts)

150 kHz to 80 MHz

80 MHz to 800 MHz

800 MHz to 2.5 GHz

⎡ 3.5 ⎤ d =⎢ ⎥ P ⎣ V1 ⎦

⎡ 3. 5 ⎤ d =⎢ ⎥ P ⎣ E1 ⎦

⎡7⎤ d =⎢ ⎥ P ⎣ E1 ⎦

0.01

0.12

0.12

0.23

0.1

0.37

0.37

0.74

1

1.17

1.17

2.33

10

3.69

3.69

7.38

100

11.67

11.67

23.33

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. Note 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies. Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

Environmental Protection

At the end of its useful life, you may return this product to Life-Tech for disposal. If you do not return it, follow your local governing ordinances and recycling plans regarding disposal or recycling of device components.

Continued on next page…

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Introduction, Continued Service

1. Damage Requiring Service: The instrument should be serviced by qualified service personnel when: • The mains AC power supply cord or the plug has been damaged. • The instrument does not appear to operate normally or exhibits a marked change in performance. • The instrument has been dropped, or the enclosure damaged. 2. Service: The user should not attempt to service the instrument beyond that described in this Operator’s Manual unless directed by Life-Tech Service personnel. Refer all other servicing to qualified service personnel. Circuit diagrams, itemized parts listings, descriptions, and other available documentation can be ordered by qualified users who are authorized by LifeTech to repair components that are designated as repairable. Supply of such technical documentation relating to the equipment shall not be construed as constituting Life-Tech’s authorization of user’s personnel, regardless of their levels of technical training, to open or repair the instrument. Explicitly exempted here from are those maintenance and repair operations described in this manual.

Meaning of Symbols

O

Off – power disconnected from mains

I

On – power connected to mains Sensitive to electro-static discharge Type BF equipment

REF

Reference (model) number

SN

Serial number Attention – consult accompanying documents. Read instructions before connecting and operating. Fuse – identifies location of fuse box Equipotential stud Rotating Machinery – hazard for fingers, hair, clothing, etc. AC voltage

IP 21

Protected against entry of foreign objects and against dripping water. Fill (rotate roller-head clockwise)

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Introduction, Continued Specifications Dimensions

3.75” (9.52 cm) W x 11.25” (28.5 cm) L x 4” (10.2 cm) H

Weight

7 pounds (4Kg), including bracket

Input Rating

100-240VAC (Auto ranging), 50 / 60Hz, 100VA

Fuses

2 x T1.0A / 250V

Infusion Rate Accuracy

± 5% or ± 1ml / min, whichever is greater.

Infusion Rates When Uropump III is connected to…

and controlled by…

the available infusion range in selected steps is…

Urolab Spectrum

Urolab Spectrum

10 - 100 ml / min

2011CU / UMC (Uropump III Manual Control)

Uropump III Manual Control

4 – 100 ml / min

2012 / 2012A Board

System III

4 – 100 ml / min

2012 / 2012A / M33-2012 Board

System IV System V

4 – 100 ml / min

M22J Patient Unit

System IV System V

4 – 100 ml / min

M30 / M30P

System V (> V1.60)

4 – 200 ml / min Continued on next page…

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Introduction, Continued Specifications (cont.)

Safety

Complies with: IEC/EN60601-1 (International/Europe) IEC/EN60601-1 C22.2 No.601.1-M90 (Canada) UL Std. No. 60601-1 (USA) Product Classification: Type BF Applied Parts Class I equipment Mode of operation: Continuous This equipment is NOT suitable for use in the presence of a flammable anesthetic mixture with air, or with oxygen, or nitrous oxide. Ingress rating: IP21

EMC

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Complies with: EN60601-1-2 (2001) (Immunity) EN61000-4-2 ESD EN61000-4-3 Radiated RF EN61000-4-4 Fast Transient/Burst EN61000-4-5 Surge EN61000-4-6 Line Conducted RF EN61000-4-8 Magnetic Fields EN61000-4-11 Line Voltage Dips (Emissions) EN61000-3-2 Line Harmonic content EN61000-3-3 Line Voltage flicker EN55011 Class B

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Accessories, Cables & Supplies Interface Cables The model of Interface Cable included with your Uropump III is based on the

control device (determines connector type) and the instrument trolley / pole set-up (determines length) you are using. Refer to the table below to identify the interface cable for your situation. WARNING: The use of cables other than those specified in this manual may result in increased emissions or decreased immunity of the Uropump III. In addition, by using a cable with the Uropump III other than those specified in this manual, it becomes the responsibility of the third-party supplier or the user of the Uropump III to determine compliance with the requirements of IEC 60601-1 when using this item. 15ft (4.5m) Cable P/N

5ft (1.5m) Cable P/N

2 ft (.6m) Cable P/N

Life-Tech Urodynamic System M30 Module

N/A

N/A

SA1761

M22J Patient Unit

N/A

SA1611

N/A

2012 / 2012A /M33-2012 Control Board

SA1625

SA1611

N/A

Urolab Spectrum

SA1625

SA1611

N/A

N/A

SA1611

N/A

When the 3011A is controlled by the…

Uropump III Manual Control

Power Cords

The model of wall power cord included with your Uropump III is primarily determined by the mains AC voltage and outlet configuration in your country. International customers requiring cordsets for 230V wall outlets should contact their local distributor for replacement power cords. Allows connection to:

P/N

100 / 120V Uropump III Power Cord

100 / 120V Wall Outlet

100 / 120V Isolation Transformer

100 / 120V UPS

SA1817

100 / 120V Hospital Grade Cordset, 3.0m

X

X

X

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Accessories, Cables & Supplies, Continued Power (Jumper) Cords

In systems that utilize a power interface with IEC plugs, a power jumper cord is included with your Uropump III (instead of a standard power cord). The model is determined by the required length of the jumper, based on the system trolley / pole configuration. Allows connection to:

P/N

100-240V Uropump III Power (Jumper) Cords

230V Isolation Transformer

M30 Module

H1667

100-240V IEC 320 Jumper Cordset, (2.5m)

X

X

H1690A

100-240V IEC 320 Jumper Cordset, (2.0m)

X

X

H1694A

100-240V IEC 320 Jumper Cordset, (1.0m)

X

X

The diagram below illustrates the various available configurations of power cord-to-power source connections:

Figure 1 – Power Cord Connections

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Accessories, Cables & Supplies, Continued The Uropump Manual Control (Model 2011CU / UMC) is used to control the pump when it cannot be attached to a Life-Tech urodynamic recording instrument. The single knob is used to set the infusion rate. The Uropump Manual Control includes the components described below:

Optional Uropump Manual Control Component

Description

Pump Control Jack

Input jack for the interface cable between the Uropump Manual Control and the Uropump III.

OFF / Infusion Rate Control Knob

In the OFF position, infusion stops. Rotate the knob clockwise to turn the pump on and to set the infusion rate of the pump. The knob’s pointer indicates the approximate infusion rate.

Power Indicator

The power indicator illuminates when the Uropump III is ON.

Figure 2 – Model 2011CU / UMC (Uropump Manual Control)

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Accessories, Cables & Supplies, Continued Tubing & Tubing Sets

You will need a supply of tubing sets for use with your Uropump III. No pump tubings other than the models listed on these pages are compatible with this pump. The tubings available for this device are described below:

 NOTE: The products listed below contain one sterile tubing or tubing set. To maintain infusion rate accuracy and for the purpose of infection control, you should replace the infusion tubing set for each new patient. Tubing Model #

Description

IPTS-LT2 / IPTSA-LT2

The Infusion Pump Tubing Set incorporates the minimum required tubing components for infusion during CMG, VLPP, and Pressure Flow. The tubing set is pre-assembled, in one sterile package.

pump tubing collar

DIPTS-LT2

The Dual Infusion Pump Tubing Set incorporates dual spikes, drip chambers, roller clamps, and the minimum required tubing components for infusion during CMG, VLPP, Pressure Flow and Cavernosography when more than one container of infusion medium is required (e.g. video urodynamics with contrast). The tubing set is pre-assembled, in one sterile package.

pump tubing collar

Figure 3 – Tubing & Tubing Sets Continued on next page…

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Accessories, Cables & Supplies, Continued Tubing & Tubing Sets (cont.) Tubing Model #

IPTS-DCLT2

Description

The Infusion Pump Tubing Set with Damping Chamber incorporates the minimum required tubing components for procedures during which you are using the Uropump III to perfuse through the pressure transmitting lumen of a catheter, such as during UPP and Whittaker tests. damping chamber pump tubing collar

infusion tube clamp

IT / ITA

The Infusion Tube is an extension tube with male luer connectors on each end. One IT / ITA is included as part of the IPTS-LT2 / IPTSA-LT2 and DIPTS-LT2 preassembled sets.

IT-RT

The Infusion Tube with Restrictor Tube is an extension tube with male luer connectors on each end and incorporates a restrictor tube for use during procedures in which the Uropump III is used to perfuse through the pressure transmitting lumen of a catheter, such as UPP and Whittaker. One IT-RT is included as part of the IPTS-DC-LT2 and DCIT-RT pre-assembled sets.

infusion tube clamp

DCIT-RT

damping chamber

The Damping Chamber / Infusion Tube with Restrictor Tube is an extension tube with male luer connectors on each end that incorporates the restrictor tube and damping chamber for use during procedures in which the Uropump III is used to perfuse through the pressure transmitting lumen of a catheter, such as UPP and Whittaker. One DCIT-RT is included as part of the IPTS-DC-LT2 pre-assembled set. infusion tube clamp

Figure 3 (cont) – Tubing & Tubing Sets Continued on next page… M1064 Rev B

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Accessories, Cables & Supplies, Continued Using a Tubing  NOTE: If you do NOT perform Whittaker or UPP procedures, skip this with Damping section. Chamber & The table below provides the recommended settings for the infusion tube clamp to Restrictor Tube obtain optimum transmission of provocation pressures and further reduce pump roller artifact when perfusing through a pressure measurement lumen. When you are…

Desired Effect

Clamp Setting

Perfusing a pressure lumen during:

Restricted

Closed

Performing a Leak Point Pressure test (cough, valsalva, crede)…

Restricted

Closed

Performing any other procedure

Unrestricted

Open

•

Resting or Stress UPP

•

Whittaker Test

 NOTE: When you are performing any other type of procedure than those listed in the table above, no restriction is required, so an open clamp is appropriate. CAUTION: With the infusion tube clamp closed, the pump tubing set is restricted. If you wish to infuse more than 20cc / minute, be sure that the restrictor tube clamp is open.

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Installation & System Interface Unpacking Uropump III Components

Attaching Uropump III to Instrument Stand

Unpack and identify all components of your Uropump III before you are ready to begin using it. As you do so, examine all parts for obvious damage. If you find any damage, observe anything unusual, or if any parts are missing, notify Life-Tech’s Technical Service Department at 800-231-9841 or 281-491-6600 before attempting to use the instrument.

WARNING: Mount the instrument on a Life-Tech instrument stand, or its equivalent, no more than 2 feet (61 cm) above the floor. Mounting the device higher than 2 feet (61 cm) could affect the stability of the pole, which may inadvertently tip over and cause damage to the instrument or injury to a person in the adjacent area. WARNING: Do NOT skip Step 4 of this procedure. The Uropump III is heavy and will easily slip and fall from the bracket if the thumbscrew underneath the bracket is not securely tightened.

„

To attach your Uropump III to the instrument stand: 1. Loosen the nylon screw on the Uropump III mounting bracket, sufficiently to allow the instrument stand to pass through. 2. Determine whether the pump will be mounted to the left or right side of the pole, then hold the bracket at the required pump operating position, and tighten the nylon screw. 3. If the tip of thumbscrew beneath the bracket protrudes above the bracket plate, back it out and then slide the Uropump III onto the bracket. 4. Tighten the thumbscrew underneath the bracket to secure the pump in place.

Figure 4 – Attaching Uropump III to Stand

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